Regulatory Affairs expertise with medicinal products for changes with impact on Product Information - Safety / Labelling changes, including CCDS creation or updatesExperience:1. 8-9 yrs of Regulatory Affairs experience in EU/UK/CH/AU/NZ: - Safety Labelling changes with impact on Product Information and management of AW updates from an RA perspective - CCDS creation or updates prior experience preferable - Change control assessments - Experience working on Centralized products is a plus 2. Veeva RIMS Knowledge. 3. Knowledge in using TVT Tool is a plus.
Job Title
Regulatory Affairs Consultant, Labelling